Abstracts - faqs.org

Abstracts

Health

Search abstracts:
Abstracts » Health

New revelations about the long-QT syndrome

Article Abstract:

The cause of one inheritable condition causing sudden heart stoppage in apparently healthy patients appears to be defects in the genes coding for ion channels in the membranes of heart muscle cells. Romano-Ward long-QT syndrome results in episodes of abnormal heart beat and sudden death. It can be treated, but is rarely diagnosed until catastrophe has struck. Recent research has identified three genetic mutations on three different chromosomes that may be found in affected families. In all three cases the gene involved codes for an ion channel in the heart membrane. The passage of ions through the cell membrane is what propagates the electrical conduction of the heartbeat. This discovery may lead to improved methods of diagnosis before symptoms appear and the development of drugs to treat the condition.

Author: Towbin, Jeffrey A.
Publisher: Massachusetts Medical Society
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1995
Genetic aspects, Ion channels

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Prolongation of the QT interval and the sudden infant death syndrome

Article Abstract:

Long-QT syndrome may cause many cases of sudden infant death syndrome (SIDS) but it may not be necessary to screen all newborn infants for this type of heart arrhythmia. A 1998 study found that 12 of 24 infants who died of SIDS had the long-QT syndrome. It may be cost-effective to screen all newborn infants at risk of SIDS with an electrocardiogram, which can detect long-QT syndrome. Even infants who test positive should not be treated immediately but screened again at 2 or 3 weeks of age and again at 2 or 3 months. Only infants who repeatedly test positive should be treated with beta-blockers.

Author: Towbin, Jeffrey A., Friedman, Richard A.
Publisher: Massachusetts Medical Society
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1998
Editorial, Complications and side effects, Risk factors, Medical examination, Infants (Newborn), Neonatal screening, Sudden infant death syndrome, Arrhythmia in children, Pediatric cardiology

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Association of viral genome with graft loss in children after cardiac transplantation

Article Abstract:

Adenovirus infection of a transplanted heart may lead to organ rejection or coronary artery disease in the transplanted heart, according to a study of 149 children. Researchers used PCR to test 553 heart biopsy samples from the children and found adenovirus in 30 out of 48 samples that tested positive for a virus.

Author: Shirali, Girish S., Ni, Jiyuan, Chinnock, Richard E., Johnston, Joyce K., Rosenthal, Geoffrey L., Bowles, Neil E., Towbin, Jeffrey A.
Publisher: Massachusetts Medical Society
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 2001
Health aspects, Causes of, Heart, Graft rejection, Heart transplantation, Adenoviruses, Human, Human adenoviruses

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Arrhythmia
Similar abstracts:
  • Abstracts: Predictive factors from cold knife conization for residual cervical intraepithelial neoplasia in subsequent hysterectomy
  • Abstracts: Implications of a 2005 measles outbreak in Indiana for sustained elimination of measles in the United States. Intussusception among infants given an oral rotavirus vaccine
  • Abstracts: TNF defined as a therapeutic target for rheumatoid arthritis and other autoimmune diseases. Neuroprotective autoimmunity -- a double-edged sword?
  • Abstracts: A novel non-invasive, in vivo technique for the quantification of leukocyte rolling and extravasation at the sites of inflammation in human patients
  • Abstracts: Raising kids in an age of affluence. Man of the house of the redefined. The family anchor
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.